A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069109



Internal ID19321894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142996055..143033553hg38UCSC Ensembl
chr6:143317192..143354690hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3837499
hg1937499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768074
SamplesKWP1
Known GenesLOC100507489
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069109
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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